Recall company profile

Abbott Medical Optics Inc. (AMO) Recalls

Overview of recall records associated with Abbott Medical Optics Inc. (AMO), including dates, categories and classifications where available.

17recall records
May 24, 2017latest record date
Sep 28, 2016earliest record date

Recall history in this database

Classification mix: Class II: 17.

Medical DeviceMay 17, 2017

AMO Healon Pro, Part No. 10270012 recall — FDA Z-2066-2017

Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.

Class IIFDA: TerminatedAbbott Medical Optics Inc. (AMO)
Medical DeviceMay 17, 2017

AMO Healon 5 Pro, Part No. 10270015 recall — FDA Z-2065-2017

Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.

Class IIFDA: TerminatedAbbott Medical Optics Inc. (AMO)
Medical DeviceMay 17, 2017

AMO Healon V, Part No. 10290045 recall — FDA Z-2067-2017

Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.

Class IIFDA: TerminatedAbbott Medical Optics Inc. (AMO)
Medical DeviceSep 28, 2016

AMO SENSAR 1-Piece IOL, Model No recall — FDA Z-2860-2016

Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they were not being checked prior to release and this may result in the release of mislabeled IOLs.

Class IIFDA: TerminatedAbbott Medical Optics Inc. (AMO)
Medical DeviceSep 28, 2016

AMO TECNIS 1-Piece IOL, Model No recall — FDA Z-2858-2016

Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they were not being checked prior to release and this may result in the release of mislabeled IOLs.

Class IIFDA: TerminatedAbbott Medical Optics Inc. (AMO)

Understanding this recall history

This page summarizes recall records in which the official source identifies Abbott Medical Optics Inc. (AMO) as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.